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Biochemical and Biophysical Research Communications
|
January 27, 2005
No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation
Ilan Salama, Stephan Hinderlich, Zipora Shlomai, et al.
The Israel Medical Association Journal : IMAJ
|
January 24, 2014
Oculopharyngeal muscular dystrophy among Bulgarian Jews: a new cluster?
Sergiu C Blumen, Anat Kesler, Ron Dabby, et al.
Neurology
|
November 16, 2012
Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis
Paloma González-Pérez, Elizabeth T Cirulli, Vivian E Drory, et al.
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Search research articles
Search
Showing results (51-60 of 53) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 53 results.
Biochemical and Biophysical Research Communications
|
January 27, 2005
No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation
Ilan Salama, Stephan Hinderlich, Zipora Shlomai, et al.
The Israel Medical Association Journal : IMAJ
|
January 24, 2014
Oculopharyngeal muscular dystrophy among Bulgarian Jews: a new cluster?
Sergiu C Blumen, Anat Kesler, Ron Dabby, et al.
Neurology
|
November 16, 2012
Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis
Paloma González-Pérez, Elizabeth T Cirulli, Vivian E Drory, et al.
Page
of 6